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Manufacturing Associate, Cell Therapy in Devens, MA

Bristol-Myers Squibb

Healthcare Jobs

Manufacturing Associate, Cell Therapy in Devens, MA

full-timePosted: Nov 5, 2025

Job Description

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team. The Manufacturing Associate, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind, with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. Shifts Available: Days: 6am - 6pm, rotating shift including holidays and weekends, onsite Nights: 6pm - 6am, rotating shift including holidays and weekends, onsite Responsibilities: Performing patient process unit operations and support operations described in standard operating procedures and batch records. Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Completing training assignments to ensure the necessary technical skills and knowledge. Assisting in setting up manufacturing areas and equipment/fixtures. Perform facility and equipment commissioning activities. Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations. Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts. Work in a cleanroom environment and perform aseptic processing; maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements. Knowledge and Skills: Driven and motivated individual to learn and execute Cell Therapy Manufacturing operations Must have the ability to work assigned shift (Day, Night, Weekends and/or Holidays). Must be able to work in a cleanroom environment and perform aseptic processing Must be comfortable being exposed to human blood components. Must be able to be in close proximity to strong magnets. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred. Basic Requirements: High school diploma and 0-2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience Bachelors in relevant science or engineering discipline is preferred Working Conditions: PHYSICAL /MENTAL DEMANDS: Stand and Walk - Required to stand/walk while operating manufacturing/computer equipment for several hours at a time, throughout the day. Carrying weight, Pushing, Pulling Lifting - Required to carry, lift, push, and/or pull up to 50 pounds several times a day while handling production equipment and/or materials. Climb - Required to climb (use of stepladders in production areas, or stairwells) several times a day. Bend and Kneel - Required to bend or kneel several times a day. Overhead work - Required to perform overhead reaching during handling of production materials/files/supplies up to 25 pounds several times a day, throughout the day. Moving Head and Neck - Required movement of head/neck while using computer applications and handling of production equipment and materials several times a day, throughout the day. Twisting - Required movement of twisting waist while setting up equipment several times a day, throughout the day. Repetitive Use - Required repetitive use of arms/wrists/hands while setting up equipment and processing several times a day, throughout the day. Will be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include, but not limited to: safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection. BMSCART LI-ONSITE GPS_2025 If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Devens - MA - US: $26.44 - $32.04per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • Bristol Myers Squibb is focused on reimagining the future of cell therapy
  • The company offers opportunities for growth and career advancement
  • BMS emphasizes a supportive culture with values of passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is committed to ensuring that people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations
  • BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters
  • BMS considers for employment qualified applicants with arrest and conviction records, pursuant to applicable laws

Key Responsibilities

  • Performing patient process unit operations and support operations described in standard operating procedures and batch records
  • Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records
  • Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements
  • Completing training assignments to ensure the necessary technical skills and knowledge
  • Assisting in setting up manufacturing areas and equipment/fixtures
  • Perform facility and equipment commissioning activities
  • Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations
  • Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts
  • Work in a cleanroom environment and perform aseptic processing
  • Maintain manufacturing environmental conditions by performing area disinfection regiment as required to meet global Health Authority requirements

Required Qualifications

  • High school diploma
  • -2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience

Preferred Qualifications

  • Bachelor's degree in a relevant science or engineering discipline
  • Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing

Skills Required

  • Driven and motivated to learn and execute Cell Therapy Manufacturing operations
  • Ability to work assigned shift (Day, Night, Weekends and/or Holidays)
  • Ability to work in a cleanroom environment and perform aseptic processing
  • Comfortable being exposed to human blood components
  • Ability to be in close proximity to strong magnets

Benefits & Perks

  • Competitive benefits, services, and programs
  • Medical, pharmacy, dental, and vision care
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • Financial well-being resources and a 401(K)
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • Work-life programs including paid national holidays, optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • Parental, caregiver, bereavement, and military leave
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • Other perks like tuition reimbursement and a recognition program

Additional Requirements

  • Must work assigned shifts including days (6am - 6pm) or nights (6pm - 6am), rotating shifts including holidays and weekends, onsite
  • Stand and walk while operating manufacturing/computer equipment for several hours at a time, throughout the day
  • Carry, lift, push, and/or pull up to 50 pounds several times a day while handling production equipment and/or materials
  • Climb using stepladders in production areas or stairwells several times a day
  • Bend or kneel several times a day
  • Perform overhead reaching during handling of production materials/files/supplies up to 25 pounds several times a day, throughout the day
  • Move head/neck while using computer applications and handling of production equipment and materials several times a day, throughout the day
  • Twist waist while setting up equipment several times a day, throughout the day
  • Repetitive use of arms/wrists/hands while setting up equipment and processing several times a day, throughout the day
  • Wear personal protective equipment (PPE) and other clean room garments daily including safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection

Locations

  • Devens MA, United States

Salary

26.44 - 32.04 USD / yearly

Skills Required

  • Driven and motivated to learn and execute Cell Therapy Manufacturing operationsintermediate
  • Ability to work assigned shift (Day, Night, Weekends and/or Holidays)intermediate
  • Ability to work in a cleanroom environment and perform aseptic processingintermediate
  • Comfortable being exposed to human blood componentsintermediate
  • Ability to be in close proximity to strong magnetsintermediate

Required Qualifications

  • High school diploma (experience)
  • -2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience (experience)

Preferred Qualifications

  • Bachelor's degree in a relevant science or engineering discipline (experience)
  • Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing (experience)

Responsibilities

  • Performing patient process unit operations and support operations described in standard operating procedures and batch records
  • Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records
  • Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements
  • Completing training assignments to ensure the necessary technical skills and knowledge
  • Assisting in setting up manufacturing areas and equipment/fixtures
  • Perform facility and equipment commissioning activities
  • Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations
  • Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts
  • Work in a cleanroom environment and perform aseptic processing
  • Maintain manufacturing environmental conditions by performing area disinfection regiment as required to meet global Health Authority requirements

Benefits

  • general: Competitive benefits, services, and programs
  • general: Medical, pharmacy, dental, and vision care
  • general: Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • general: Financial well-being resources and a 401(K)
  • general: Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • general: Work-life programs including paid national holidays, optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • general: Parental, caregiver, bereavement, and military leave
  • general: Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • general: Other perks like tuition reimbursement and a recognition program

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Bristol-Myers Squibb logo

Manufacturing Associate, Cell Therapy in Devens, MA

Bristol-Myers Squibb

Healthcare Jobs

Manufacturing Associate, Cell Therapy in Devens, MA

full-timePosted: Nov 5, 2025

Job Description

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team. The Manufacturing Associate, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind, with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. Shifts Available: Days: 6am - 6pm, rotating shift including holidays and weekends, onsite Nights: 6pm - 6am, rotating shift including holidays and weekends, onsite Responsibilities: Performing patient process unit operations and support operations described in standard operating procedures and batch records. Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Completing training assignments to ensure the necessary technical skills and knowledge. Assisting in setting up manufacturing areas and equipment/fixtures. Perform facility and equipment commissioning activities. Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations. Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts. Work in a cleanroom environment and perform aseptic processing; maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements. Knowledge and Skills: Driven and motivated individual to learn and execute Cell Therapy Manufacturing operations Must have the ability to work assigned shift (Day, Night, Weekends and/or Holidays). Must be able to work in a cleanroom environment and perform aseptic processing Must be comfortable being exposed to human blood components. Must be able to be in close proximity to strong magnets. Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred. Basic Requirements: High school diploma and 0-2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience Bachelors in relevant science or engineering discipline is preferred Working Conditions: PHYSICAL /MENTAL DEMANDS: Stand and Walk - Required to stand/walk while operating manufacturing/computer equipment for several hours at a time, throughout the day. Carrying weight, Pushing, Pulling Lifting - Required to carry, lift, push, and/or pull up to 50 pounds several times a day while handling production equipment and/or materials. Climb - Required to climb (use of stepladders in production areas, or stairwells) several times a day. Bend and Kneel - Required to bend or kneel several times a day. Overhead work - Required to perform overhead reaching during handling of production materials/files/supplies up to 25 pounds several times a day, throughout the day. Moving Head and Neck - Required movement of head/neck while using computer applications and handling of production equipment and materials several times a day, throughout the day. Twisting - Required movement of twisting waist while setting up equipment several times a day, throughout the day. Repetitive Use - Required repetitive use of arms/wrists/hands while setting up equipment and processing several times a day, throughout the day. Will be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include, but not limited to: safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection. BMSCART LI-ONSITE GPS_2025 If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Devens - MA - US: $26.44 - $32.04per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • Bristol Myers Squibb is focused on reimagining the future of cell therapy
  • The company offers opportunities for growth and career advancement
  • BMS emphasizes a supportive culture with values of passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is committed to ensuring that people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations
  • BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters
  • BMS considers for employment qualified applicants with arrest and conviction records, pursuant to applicable laws

Key Responsibilities

  • Performing patient process unit operations and support operations described in standard operating procedures and batch records
  • Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records
  • Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements
  • Completing training assignments to ensure the necessary technical skills and knowledge
  • Assisting in setting up manufacturing areas and equipment/fixtures
  • Perform facility and equipment commissioning activities
  • Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations
  • Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts
  • Work in a cleanroom environment and perform aseptic processing
  • Maintain manufacturing environmental conditions by performing area disinfection regiment as required to meet global Health Authority requirements

Required Qualifications

  • High school diploma
  • -2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience

Preferred Qualifications

  • Bachelor's degree in a relevant science or engineering discipline
  • Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing

Skills Required

  • Driven and motivated to learn and execute Cell Therapy Manufacturing operations
  • Ability to work assigned shift (Day, Night, Weekends and/or Holidays)
  • Ability to work in a cleanroom environment and perform aseptic processing
  • Comfortable being exposed to human blood components
  • Ability to be in close proximity to strong magnets

Benefits & Perks

  • Competitive benefits, services, and programs
  • Medical, pharmacy, dental, and vision care
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • Financial well-being resources and a 401(K)
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • Work-life programs including paid national holidays, optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • Parental, caregiver, bereavement, and military leave
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • Other perks like tuition reimbursement and a recognition program

Additional Requirements

  • Must work assigned shifts including days (6am - 6pm) or nights (6pm - 6am), rotating shifts including holidays and weekends, onsite
  • Stand and walk while operating manufacturing/computer equipment for several hours at a time, throughout the day
  • Carry, lift, push, and/or pull up to 50 pounds several times a day while handling production equipment and/or materials
  • Climb using stepladders in production areas or stairwells several times a day
  • Bend or kneel several times a day
  • Perform overhead reaching during handling of production materials/files/supplies up to 25 pounds several times a day, throughout the day
  • Move head/neck while using computer applications and handling of production equipment and materials several times a day, throughout the day
  • Twist waist while setting up equipment several times a day, throughout the day
  • Repetitive use of arms/wrists/hands while setting up equipment and processing several times a day, throughout the day
  • Wear personal protective equipment (PPE) and other clean room garments daily including safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection

Locations

  • Devens MA, United States

Salary

26.44 - 32.04 USD / yearly

Skills Required

  • Driven and motivated to learn and execute Cell Therapy Manufacturing operationsintermediate
  • Ability to work assigned shift (Day, Night, Weekends and/or Holidays)intermediate
  • Ability to work in a cleanroom environment and perform aseptic processingintermediate
  • Comfortable being exposed to human blood componentsintermediate
  • Ability to be in close proximity to strong magnetsintermediate

Required Qualifications

  • High school diploma (experience)
  • -2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing or relevant experience (experience)

Preferred Qualifications

  • Bachelor's degree in a relevant science or engineering discipline (experience)
  • Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing (experience)

Responsibilities

  • Performing patient process unit operations and support operations described in standard operating procedures and batch records
  • Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records
  • Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements
  • Completing training assignments to ensure the necessary technical skills and knowledge
  • Assisting in setting up manufacturing areas and equipment/fixtures
  • Perform facility and equipment commissioning activities
  • Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations
  • Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts
  • Work in a cleanroom environment and perform aseptic processing
  • Maintain manufacturing environmental conditions by performing area disinfection regiment as required to meet global Health Authority requirements

Benefits

  • general: Competitive benefits, services, and programs
  • general: Medical, pharmacy, dental, and vision care
  • general: Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • general: Financial well-being resources and a 401(K)
  • general: Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • general: Work-life programs including paid national holidays, optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
  • general: Parental, caregiver, bereavement, and military leave
  • general: Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • general: Other perks like tuition reimbursement and a recognition program

Target Your Resume for "Manufacturing Associate, Cell Therapy in Devens, MA" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Manufacturing Associate, Cell Therapy in Devens, MA. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Manufacturing Associate, Cell Therapy in Devens, MA" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Answer 10 quick questions to check your fit for Manufacturing Associate, Cell Therapy in Devens, MA @ Bristol-Myers Squibb.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

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No related jobs found at the moment.